Nitromethylene derivatives and their use

ABSTRACT

The present invention discloses nitromethylene derivatives and the uses thereof. These derivatives are obtained by adding ring structure onto the known nitromethylene compounds, by which both their stability for light and their liposolubility are increased. Furthermore, by using the substituents linked to ether bond, the steric orientation of the nitro group and the liposolubility of the compounds are controlled. The insecticidal activity tests show that the compounds and their derivatives of the invention display high efficiency on killing various destructive insects with piercing-sucking type or scratching type mouthparts, such as aphid, leafhopper, plant hpooer, thrips and white fly.

CROSS-REFERENCE TO RELATED APPLICATIONS

This application is a continuation of International application number PCT/CN2005/000617, filed Apr. 30, 2005 which claims priority to Chinese application No. CN 200410084457.1 filed Nov. 23, 2004, the contents of both are herein incorporated in their entirety by reference.

FIELD OF THE INVENTION

This invention relates to nitromethylene derivatives and the uses thereof.

BACKGROUND OF THE INVENTION

Alkaloid nicotine is a natural insecticide from the extraction of tobacco leaves, and it acts on the postsynaptic nicotinic acetylcholine receptor (nAchRs). By so far, using natural nicotine as a leading compound, researchers have been making efforts to look for and develop a new insecticidally active compound having a similar structure and the same mechanism of action as nicotine. Since Soloway et al firstly reported the insecticidally active nitromethylene heterocyclic compounds in 1978, researchers have been changing the functional groups of nitromethylene heterocyclic compounds and Bayer AG successfully developed the first nicotine insecticide—Imidacloprid in middle 1980s. Due to its unique mechanism of action, no mutual resistance with common insecticides, high effect, broad spectrum, good root systemic ability, contact toxicity, stomach toxicity, low toxicity to mammalian, and safety to the environment, this kind of nicotine insecticide catches people's attention at once. A series of nicotine insecticide such as Thiacloprid, Clothianidin, Thiamethoxam, Acetamiprid, Nitenpyram and Dinotefuran are developed (EP 247477, 296453, 685477, 235725, 235725, 315826, 192060, 244777, 0386565, 580553, 1031566,JP 62292765, 8259568, 8291171, 7242633).

Compared to Imidacloprid, nitromethylene compounds have higher binding affinity and insecticidal activity. Whereas its use as an insecticide has been restricted by its instability to light and low LogP value. Therefore, the technical problem to be solved by the present invention is how to structurally modify the highly active nitromethylene compound to make it useful as an insecticide.

SUMMARY OF THE INVENTION

The object of this invention is to provide a kind of nitromethylene derivatives and the uses thereof.

Based on the current nitromethylene compound, this invention adds a new ring to its structure in order to enhance its light stability and liposolubility. Furthermore, this invention can control the space orientation and liposolubility by the substituent linked to an ether bond.

According to the first aspect of this invention, it is provided a nitromethylene derivative of formula (I), or an agriculturally acceptable salt thereof.

wherein R₁ is a substituted or unsubstituted 5- or 6-membered heterocycle containing nitrogen, oxygen and/or sulfur, the substituents are one to three substituents selected from the group consisting of a halogen atom, C₁₋₄ haloalkyl and C₁₋₄ haloalkoxyl;

R₂ is a hydrogen atom, a saturated or unsaturated C₁₋₈ hydrocarbyl group, a saturated or unsaturated C₁₋₈ halogenated hydrocarbyl group, —CH₂CH₂OCH₂CH₃, —CH₂CH₂OCH₃, a substituted or unsubstituted phenyl group, a substituted or unsubstituted benzyl group, a substituted or unsubstituted C₁₋₈ alkoxyl group which may be saturated or unsaturated, wherein the substituents are one to three substituents selected from the group consisting of a halogen atom, C₁₋₄ haloalkyl and C₁₋₄ haloalkoxyl;

or R₂ is a group of the following formula:

wherein Ra is methyl, trifluoromethyl or phenyl; Rb is methyl, trifluoromethyl, pyridyl, phenyl or phenyl substituted by a halogen atom and/or a nitro group;

R₃ and R₄ independently is hydrogen, a substituted or unsubstituted C₁₋₃ alkyl group, wherein the substituents are one to three substituents selected from the group consisting of halogen, C₁₋₄ haloalkyl and C₁₋₄ haloalkoxyl;

A is O, S or N;

n is 0 or 1.

Preferably, R₁ is one of pyridyl, thiazolyl, pyrimidinyl, tetrahydrofuryl, oxazolyl, or halide thereof (especially chloride); R₂ is saturated or unsaturated C₁₋₈ hydrocarbyl, saturated or unsaturated C₁₋₈ halogenated hydrocarbyl, —CH₂CH₂OCH₂CH₃, —CH₂CH₂OCH₃, a saturated or unsaturated C₁₋₈ alkoxyl group; R₃ is hydrogen or methyl; R₄ is hydrogen or C₁₋₃ alkyl group.

One kind of especially preferable compound has the structure of formula II (i.e. R₃=R₄=H, n=0):

wherein R₁, R₂ and A are defined as above.

More preferably, R₁ represents

More preferably, R₂ is saturated or unsaturated C₁₋₅ hydrocarbyl group, a saturated or unsaturated C₁₋₅ hydrocarbyl group which may be substituted by halogen (such as fluorine or chlorine), —CH₂CH₂OCH₂CH₃, —CH₂CH₂OCH₃, saturated or unsaturated C₁₋₈ alkoxyl group.

More preferably, A is O or S.

According to the second aspect of this invention, it is provided the use of the nitromethylene derivatives or the salts thereof to prepare chemical insecticide for agriculture.

According to the third aspect of this invention, it is provided an insecticidal composition comprising an effective amount of the compound of the present invention or an agriculturally acceptable salt thereof in mixture with an agriculturally acceptable carrier or diluent.

The nitromethylene derivatives can be synthesized by the following scheme:

In one of the preferable example, the ether derivatives containing a nitromethylene structure can be prepared by the following steps:

(1): A mixture of nitromethane and carbon bisulfide dissolved in alcohols is added dropwise to the solution of potassium hydroxide in alcohol at room temperature. The reaction is carried out at the temperature range of 0-35° C. for 2-10 hours. The solid is filtered out to afford a crude product potassium 2-nitroethene-1,1-bis(thiolate) which is a brown yellow powder.

(2): Potassium 2-nitroethene-1,1-bis(thiolate) is dissolved in alcohol, and then to the resulting mixture is added dropwise dimethyl sulfate solution. The reaction is stirred at room temperature for 2-8 hours. The mixture is filtrated to obtain crude product 1,1 -dimethylthio-2-nitroethene, which is a light brown yellow powder.

(3): The solution of 2-chloro-5-(chloromethyl)pyridine in acetonitrile is added dropwise to 5-10 mole of diamine solution. The reaction is carried out at the temperature range of 0-50° C. for 5-10 hours. The mixture is distillated under reduced pressure to remove diamine, and then dissolved in ethyl acetate and evaporated to obtain N¹-((6-chloropyridin-3-yl)methyl)diamine

(4): The mixture of N¹-((6-chloropyridin-3-yl)methyl) diamine and 1,1-dimethylthio-2-nitroethene is dissolved in ethanol and refluxed for 4-8 hours to obtain the product nitromethylene compound.

(5): In the presence of a acid catalyst such as hydrochloric acid, sulfuric acid, acetic acid, trifluoroacetic acid and the like, nitromethylene compound reacts with acraldehyde to obtain a new nitromethylene compound having hydroxyl.

In the presence of a catalytic amount of acid catalyst such as hydrochloric acid, sulfuiric acid, acetic acid, trifluoroacetic acid and the like, the mixture of the new nitromethylene compound having hydroxyl and various alcohols is refluxed to obtain the target compound.

In the presence of a catalytic amount of acid catalyst such as Lewis acid, such as trifluoroboric acid, aluminum trichloride, and the like, the mixture of the new nitromethylene compound having a hydroxyl and various mercaptans is refluxed to obtain the target compound.

In the presence of an acid-binding agent such as organic or inorganic alkali, for example pyridine, triethylamine, potassium carbonate, potassium hydroxide and the like, the mixture of the new nitromethylene compound having hydroxyl and various acyl chlorides is refluxed to obtain the target compound.

In another preferable example, the Schiff's base derivatives of nitromethylene compound can be prepared by the following steps:

(1) The mixture of nitromethylene compound and methyl acrylate reacts at 0-100° C. to obtain a new nitromethylene compound bearing carbonyl group;

(2) The mixture of the new nitromethylene compound with carbonyl group and hydroxylamine is refluxed to obtain new Schiffs base derivatives of nitromethylene compound

The Schiff's base derivatives of nitromethylene compound can react with halogen substituted alkanes to obtain the target compound in the presence of organic or inorganic alkali such as sodium hydride, sodium methoxide, sodium ethoxide, potassium hydroxide and the like.

The Schiff's base derivatives of nitromethylene compound can react with various acyl chlorides to obtain the target compound in the presence of an acid-binding agent such as organic or inorganic alkali, for example pyridine, triethylamine, potassium carbonate, and the like.

The invention is further illustrated by the following examples. It should be appreciated that these examples are only intended to illustrate the invention, but not to limit the scope of the invention. For the experimental methods in the following examples, they are performed under routine conditions, or as instructed by the manufacturers, unless otherwise specified.

EXAMPLE 1 Synthesis of 1-((6-chloropyridin-3-yl)methyl)-8-nitro-1,2,3,5,6,7-hexahydro imidazo[1,2-a]pyridin-5-ol (compound 1) (1) Synthesis of potassium 2-nitro-ethene-1,1-bis(thiolate)

4 g (0.03 mol) of nitromethane and 6 ml (0.05 mol) of carbon bisulfide were placed in a 100 ml three-necked flask and 10 ml of ethanol was added as a solvent, and then the solution was stirred. To the resulting solution was added slowly and dropwise the solution of 8 g (0.14 mol) of potassium hydroxide in 40 ml of ethanol at room temperature over nearly 30 min. Since the reaction was exothermic, the rate of addition depended on the reaction temperature which was preferably between 30-35° C. After the addition was complete, the mixture was further stirred for 2 hours, filtered to obtain a crude product, which was a brown yellow powder in 72% yield.

(2): Synthesis of 1,1-dimethylthio-2-nitroethene

To a solution of 2 g (0.0094 mol) of potassium 2-nitroethene-1,1-bis(thiolate) in 10 ml of dried methanol, 0.0187 mol of dimethyl sulphate was added. The mixture was then stirred for 2 hours at room temperature. The precipitated solid was filtered to obtain crude product, which was a light brown yellow powder in 70% yield.

GC/ MS(m/s) 165 (31) M⁺,148(17), 104(66), 86(100), 72(93), 57(20).

(3): Synthesis of N¹-((6-chloropyridin-3-yl)methyl)ethane-1,2-diamine

To a stirred solution of 4.2 g (0.03 mol) of potassium carbonate and 10 ml (0.15 mol) of ethylenediamine in a 50 ml of flask placed in an ice bath, 4.8 g (0.03mol) of 2-chloro-5-(chloromethyl)pyridine dissolved in 15 ml of acetonitrile was added dropwise and slowly for nearly 20 min. After addition, the ice bath was removed and then the mixture was stirred for 8 hours at room temperature. After the reaction was stopped, a large amount of water was added to dissolve potassium carbonate and ethylenediamine, and the mixture was extracted with dichlormethane. The lower organic phase was collected, dried, and evaporated to dryness (It was better to remove all of the ethylenediamine in the solvent since its presence would influence the following step). The obtained product was yellow oily liquid in 68% yield.

GC MS(m/s) 185 (5) M⁺, 155(49), 126(100), 99(9), 90(12).

(4): Synthesis of 2-chloro-5-((2-(nitromethylene)imidazolidin-1-yl)methyl) pyridine

2.5 g (0.0178 mol) of 1,1-dimethylthio-2-nitroethene, 3.3g (0.0178 mol) of N¹-((6-chloropyridin-3-yl)methyl)ethane-1,2-diamine were added to 15 ml of ethanol. The resulting mixture was heated under reflux for 4 hours at 80-90° C. The mixture was then cooled to educe solid, concentrated, filtrated and dried to give a light yellow powder in 56% yield.

R_(f)=0.46 (petroleum ether: ethyl acetate =1:1).

Mp=156.9° C.-161.8° C. GC MS (m/s) 220 (25), 126(100), 90(9).

(5): Synthesis of 1-((6-chloropyridin-3-yl)methyl)-8-nitro-1,2,3,5,6,7-hexahydro imidazo[1,2-a]pyridin-5-ol

A mixture of 0.509 g (0.002 mol) of 2-chloro-5-((2-(nitromethylene)imidazolidin-1-yl)methyl)pyridine, 15 ml of anhydrous acetonitrile, 0.15 ml of acrylaldehyde and a catalytic amount of HCl place in a 50 ml of flask was heated to 40° C. and the mixture was kept at 40° C. and stirred for 12 hours. After the reaction was stopped, the precipitated solid was filtrated to give a crude product. After recrystallization, the pure product was a yellow powder in 40% yield.

Mp=169.0-172.1° C.

IR (KBr, cm⁻¹) 3190, 1560, 1520, 1370, 1300, 1150, 970, 590.

¹HNMR (CDCl₃), δ (ppm)500 MHz: 8.37(d, J=2 Hz, 1H, Py-H), 7.85(dd, J₁=2 Hz, J₂=8.29 Hz, 1H, Py-H), 7.41(d, J=8 Hz, 1H, Py-H), 6.33(d, J=5.47 Hz, 1H, —OH), 4.86(m, 1H, —CHOH), 4.65(dd, J₁=J₂=15 Hz, 2H, —CH₂-N—), 3.52(m, 4H, imidazolidine-H), 2.60(m, 2H, —CH₂CH₂—), 1.79(m, 2H, —CH₂CH₂—).

GC MS (m/s) 220 (25), 126(100), 90(9).

Elementary analysis Calculated: C 50.25, H 4.87, N 18.03; found C 50.12, H 4.82, N 18.31

EXAMPLE 2 Synthesis of 1-((6-chloropyridin-3-yl)methyl)-5-methoxy-8-nitro-1,2,3,5,6,7-hexahydroimidazo[1,2-a]pyridine (compound 2)

0.31 g (0.0001 mol) of compound 1 was added to a 50 ml of round-bottomed flask, and 15 ml of methanol and a catalytic amount of glacial acetic acid were added. The resulting mixture was refluxed and followed by TLC. After the reaction was stopped, the solvent was removed. The residue was then separated to give a pure yellow powder by column chromatography in 90% yield.

Mp=154.0-155.4° C.

IR (KBr, cm⁻¹) 2900, 1560, 1350, 1080, 900, 760, 590

¹H NMR (CDCl₃), δ (ppm) 500 MHz: 8.32(d, J=2 Hz, 1H, Py-H), 7.88(dd, J₁=2 Hz, J₂=8 Hz, 1H, Py-H), 7.35(d, J=8 Hz, 1H, Py-H), 4.78(d, J₁=15 Hz, J₂=15 Hz, 2—CH₂—N—), 4.48(t, J₁=3 Hz,J₂=3 Hz, 1H, —CHO—), 3.60(m, 4H, imidazolidine-H), 3.19(m, 3H, —OCH₃), 2.90(m, 2H, —CH₂CH₂—), 1.95(m, 2H, —CH₂CH₂—)

Elementary analysis Calculated: C 51.78, H 5.28, N 17.25; found C 51.95, H 5.12, N 17.04

EXAMPLE 3 Synthesis of 1-((6-chloropyridin-3-yl)methyl)-5-ethoxy-8-nitro-1,2,3,5,6,7-hexahydroimidazo[1,2-a]pyridine(compound 3)

Following the steps described in example 2, except that ethanol was used instead of methanol, a pure yellow powder was obtained by column chromatography in 85% yield.

Mp=126.4-128.1° C. IR (KBr) 3050 m, 2870 m, 1570 vs, 1500s, 1310 vs, 1150vs, 1030s, 970 m, 760 m, 580 m cm⁻¹ ¹H NMR (CDCl₃) δ (ppm) 500 MHz=8.33(d, J=2 Hz, 1H, Py-H), 7.91(dd, J₁=2 Hz, J₂=2 Hz, 1H, Py-H), 7.33(d, J=8 Hz, 1H, Py-H), 4.78(d, J₁=15 Hz, J₂=15 Hz, 2H, —CH₂—N—), 4.54(t, J₁=3 Hz, J₂=3 Hz, 1H, —CHO—), 3.68(m, 2H, —O—CH₂—), 3.57(m, 4H, imidazolidine-H), 2.87 (m, 2H, —CH₂CH₂—), 1.89(m, 2H, —CH₂CH₂—), 1.23(t, J₁=7 Hz, J₂=7 Hz, 3H, —CH₃)

Elementary analysis Calculated: C 53.18, H 5.65, N 17.54; found C 53.64,H 5.57, N 17.68

EXAMPLE 4 Synthesis of 1-((6-chloropyridin-3-yl)methyl)-5-propoxy-8-nitro- 1,2,3,5,6,7-hexahydroimidazo[1,2-a]pyridine (compound 4)

Following the steps described in example 2, except that propanol was used instead of methanol, a pure yellow powder was obtained by column chromatography in 78% yield.

Mp=115.71-117.6° C.

IR (KBr cm⁻¹) 2900, 2370, 1580, 1500, 1310, 1150, 1090, 1000, 820

¹H NMR (CDCl₃) δ (ppm) 500 MHz : 8.37(d, J=2 Hz, 1H, Py-H), 7.89(dd, J₁=2 Hz, J₂=2 Hz, 1H, Py-H), 7.32(d, J=8 Hz, 1H, Py-H), 4.77(d, J₁=15 Hz, J₂=15 Hz, 2H,—CH₂—N—), 4.56(t, J₁=3 Hz, J₂=3 Hz, 1H, —CHO—), 3.68(m, 2H, —O—CH₂—), 3.57(m, 4H, imidazolidine-H), 2.84 (m, 2H, —CH₂CH₂—), 1.89(m, 2H, —CH₂CH₂—), 1.68(m, 2H, —CH₂CH₃), 0.93(t,3H,—CH₃)

Elementary analysis Calculated: C 54.47, H 6.00, N 15.88; found C 54.62, H 5.98, N 15.54

EXAMPLE 5 Synthesis of 1-((6-chloropyridin-3-yl)methyl)-5-isopropoxy-8-nitro-1,2,3,5,6,7-hexahydroimidazo[1,2-a]pyridine (compound 5)

Following the steps described in example 2, except that propan-2-ol was used instead of methanol, a pure yellow powder was obtained by column chromatography in 80% yield.

Mp=129.9-134.6 ° C.

IR (KBr cm⁻¹) 2900, 2370, 1560, 1330, 1200, 1120, 1070, 1000, 970, 820, 590

¹H NMR (CDCl₃) δ (ppm) 500 MHz: 8.32(d, J=2 Hz, 1H, Py-H), 7.91(dd,J₁=2 Hz, J₂=2 Hz, 1H, Py-H), 7.31(d, J=8 Hz, 1H, Py-H), 4.76(d, J₁=15 Hz,J₂=15 Hz, 2H, —CH₂—N—), 4.59(t, J₁=3 Hz, J₂=3 Hz, 1H, ——CHO—), 3.72 (m, 2H, —O—CH—), 3.69(m, 4H, imidazolidine-H), 2.89(m, 2H, —CH₂CH2—), 1.87(m, 2H, —CH₂CH₂—), 1.21(m, 6H, —(CH₃)₂)

Elementary analysis Calculated: C 54.47, H 6.00, N 15.88; found C 54.52, H 5.84, N 15.90

EXAMPLE 6 Synthesis of 1-((6-chloropyridin-3-yl)methyl)-8-nitro-5-pentyloxy-1,2,3,5,6,7-hexahydroimidazo[1,2-a]pyridine (compound 6)

Following the steps described in example 2, except that pentanol was used instead of methanol, a pure yellow powder was obtained by column chromatography in 75% yield.

Mp=83.5-85.2° C.

IR (KBr cm⁻¹)2900, 2720, 1670, 1550, 1440, 1330, 1150, 1080, 980, 810, 750, 590

¹H NMR (CDCl₃) δ (ppm) 500 MHz : 8.33(d, J=2 Hz, 1H, Py-H), 7.92(dd, J₁=2 Hz, J₂=8 Hz, 1H, Py-H), 7.31(d J=8 Hz, 1H, Py-H), 4.77(d, J₁=15 Hz, J₂=15 Hz, 2H, —CH2—N—), 4.59(s, 1H, —CHO—), 3.68(m, 2H, —O—CH2—), 3.51(m, 4 H, imidazolidine-H), 2.86(m, 2H, —CH2CH2—), 1.95(m, 2H, —CH2CH2—), 1.58(m, 2H, —O—(CH2)3—), 1.32(m, 4H, —O—(CH2)3—), 0.92(t,3H,—CH3)

Elementary analysis Calculated: C 57.76, H 6.62, N 14.71; found C 57.68, H 6.45, N 14.42

EXAMPLE 7 Synthesis of 5-(2-chloroethoxy)- 1 -((6-chloropyridin-3 -yl)methyl)-8-nitro-1,2,3,5,6,7-hexahydroimidazo[1,2-a]pyridine (compound 7)

Following the steps described in example 2, except that 2-chloroethanol was used instead of methanol, a pure yellow powder was obtained by column chromatography in 79% yield.

Mp=158.5-159.4° C.

IR (KBr cm⁻¹) 3000, 2370, 1560s, 1350, 1280, 1130

¹H NMR (CDCl₃) δ (ppm) 500 MHz: 8.33(d, J=2 Hz, 1H, Py-H), 7.91(dd, J₁=2 Hz, J₂=8 Hz, 1H, Py-H), 7.32(t, J=8 Hz, 1H, Py-H), 4.75(d, J₁=15 Hz, J₂=15 Hz, 2H, —CH₂—N—), 4.66(t, J₁=3 Hz, J₂=3 Hz, 1H, —CHO—), 3.85(m, 4H, —O—(CH₂)₂—), 3.57(m, 4H, imidazolidine-H), 2.88 (m, 2H, —CH₂CH₂—), 1.93(m, 2H, —CH₂CH₂—)

Elementary analysis Calculated: C 48.27, H 4.86, N 15.01; found C 48.47, H 4.95, N 14.40

EXAMPLE 8 Synthesis of 1-((6-chloropyridin-3-yl)methyl)-9-nitro-2,3,4,6,7,8-hexahydro-1H-pyrido[1,2-a]pyrimidin-6-ol (compound 8) (1): Synthesis of N¹-((6-chloropyridin-3-yl)methyl)propane-1,3-diamine

To a stirred solution of 2.07 g (0.015 mol) of potassium carbonate and 6.25 ml (0.075 mol) of propane-1,3-diamine in a 50 ml of flask placed in an ice bath, 2.42 g (0.015 mol) of 2-chloro-5-(chloromethyl)pyridine dissolved in 15 ml of acetonitrile was added dropwise and slowly for nearly 20 min. After addition, the ice bath was removed and then the mixture was stirred at room temperature for 8 hours. After the reaction was stopped, a large amount of water was added to dissolve potassium carbonate and propane-1,3-diamine, and the mixture was extracted with dichlormethane. The lower organic phase was collected, dried, and evaporated to dryness (It was better to remove all of the propane-1,3-diamine in the solvent since its presence would influence the following step). The obtained product was yellow oily liquid in 68% yield.

GC MS(m/s) 199 (5) M⁺, 182(10), 167(12), 155(17), 141(24), 126(100), 99(10), 90(13), 73(25), 56(10).

(2): Synthesis of 1-((6-chloropyridin-3-yl)methyl)-2-(nitromethylene)hexahydro pyrimidine

2.5 g (0.0178 mol) of 1,1-dimethylthio-2-nitroethene, 3.6 g (0.0178 mol) of N¹-((6-chloropyridin-3-yl)methyl)propane-1,3-diamine were added to 15 ml of ethanol. The resulting mixture was heated under reflux for 4 hours at 80-90 ° C. The mixture was then cooled to educe solid, concentrated, filtrated and dried to give light yellow powder in 56% yield.

R_(f)=0.19 (ethanol: dichlormethane =1:1)

Mp=175.7° C.-182.6° C.

GC MS (m/s) 225(100), 196(9), 154(10), 139(11), 126(31), 113(10), 99(31)

(3): Synthesis of 1-((6-chloropyridin-3-yl)methyl)-9-nitro-2,3,4,6,7,8-hexahydro -1H-pyrido[1,2-a]pyrimidin-6-ol

The preparation method was the same as that of example 1, except using 1-((6-chloropyridin-3-yl)methyl)-2-(nitromethylene)hexahydropyrimidine as a starting material. The reaction was stopped and the precipitated solid was filtrated to give a crude product, which was recrystallized to give the pure product in 51 % yield.

Mp=172.7-173.9° C.

IR (KBr, cm⁻¹) 2900, 2370, 1680, 1560, 1400, 1340, 1140, 980, 750, 590

¹HNMR (CDCl₃) δ (ppm) 500 MHz: 8.28(d, J=2 Hz, 1H, Py-H), 7.74(dd,J=2 Hz, J₂=2Hz 1H, Py-H), 7.48(d, J=8Hz, 1H, Py-H), 6.37(s, 1H, —OH), 4.82(s, 1H, —CHOC), 4.46(d,J₁=15 Hz, J₂=15 Hz, 2H, —CH₂—N—), 2.93(m, 4H, pyrimidine-H), 1.83(m, 2H, pyrimidine-H, 2H, —CH₂CH₂—), 1.07(m, 2H, —CH₂CH₂—). GC MS (m/s) 225(100), 196(9) 154(10), 139(11), 126(31), 113(10), 99(31)

Elementary analysis Calculated: C51.78, H 5.28, N 17.25; found C 52.92, H 5.36, N 17.11

EXAMPLE 9 Synthesis of 1-((2-chlorothiazol-5-yl)methyl)-8-nitro- 1,2,3,5,6,7-hexahydro imidazo[1,2-a]pyridin-5-ol (compound 9) (1): Synthesis of N¹-((2-chlorothiazol-5-yl)methyl)ethane-1,2-diamine

To a stirred solution of 0.03 mol of potassium carbonate and 10 ml (0.15 mol) of ethylenediamine in a 50 ml of flask placed in an ice bath, 0.03 mol of 2-chloro-5-(chloromethyl)thiazole dissolved in 15 ml of acetonitrile was added dropwise and slowly. After addition, the ice bath was removed and then the mixture was stirred for 8 hours at room temperature. After the reaction was stopped, a large amount of water was added to dissolve potassium carbonate and ethylenediamine, and the mixture was extracted with dichlormethane. The lower organic phase was collected, dried, and evaporated to dryness. The obtained product was yellow oily liquid in 70% yield.

GC MS (m/s) 191 (21) M⁺, 132(100).

(2): Synthesis of 1-((2-chlorothiazol-5-yl)methyl)-2-(nitromethylene)- 1-imidazolidine

2.5 g (0.0178 mol) of 1,1-dimethylthio-2-nitroethene, 3.3 g (0.0178 mol) of N¹-((2-chlorothiazol-5-yl)methyl)ethane-1,2-diamine were added to 15 ml of ethanol. The resulting mixture was heated under reflux for 4 hours at 80-90° C. The mixture was then cooled to educe solid, concentrated, filtrated and dried to give a light yellow powder in 56% yield.

GC MS(m/s) 226 (24), 132(100), 77(9).

(3): Synthesis of 1 -((2-chlorothiazol-5-yl)methyl)-8-nitro- 1,2,3,5,6,7-hexahydroimidazo [1,2-a]pyridin-5-ol

A mixture of 0.002 mol of 1-((2-chlorothiazol-5-yl)methyl)-2-(nitromethylene) imidazolidine, 15 ml of anhydrous acetonitrile, 0.15 ml of acrylaldehyde and a catalytic amount of HCl place in a 50 ml of flask was heated to 40° C. and the mixture was kept at 40° C. and stirred for 12 hours. The precipitated solid was filtrated to give a crude product. After recrystallization, the pure product was a yellow powder in 40% yield.

Mp=172-174.6° C.

IR (KBr, cm⁻¹) 3194, 1564, 1545, 1373, 1310, 1150

Elementary analysis Calculated: C47.71, H 4.14, N 17.69; found C 47.89, H 4.35, N 17.45

EXAMPLE 10 Synthesis of 1-((2-chlorothiazolyl-5-yl)methyl)-5-ethoxy-8-nitro-1,2,3,5,6,7-hexahydroimidazo[1,2-a]pyridine (compound 10)

0.001 mol of compound 9 was added to a 50 ml of round-bottomed flask, and then 15 ml of methanol and a catalytic amount of glacial acetic acid were added. The resulting mixture was refluxed and followed by TLC. After the reaction was stopped, the solvent was removed. The residue was then separated to give a pure yellow powder by column chromatography in 85% yield.

Mp=128.4-129.2° C.

IR (KBr) 3052 m, 2872 m, 1573 vs, 1503s, 1312 vs, 1150vs, 1030s cm⁻¹,

Elementary analysis Calculated: C 45.28, H 4.97, N 16.25; found C 45.19, H 4.92, N 16.56

EXAMPLE 11 Synthesis of 8-nitro-1-((tetrahydrofuran-3-yl)methyl)-1,2,3,5,6,7-hexahydro imidazo[1,2-a]pyridin-5-ol (compound 11) (1): Synthesis of N¹-((tetrahydrofuran-3-yl)methyl)ethane-1,2-diamine

A mixture of 0.2 mol of 3-(chloromethyl)tetrahydrofuran, 200 ml of ethanol, 0.2 mol of potassium carbonate and 0.2 mol of ethylenediamine placed in a 500 ml of round-bottomed flask was refluxed for 24 hours, and then the solvent was removed. The obtained product was yellow oily liquid in 77% yield.

GC MS (m/s) 144 (67), 99(100)

(2): Synthesis of 2-(nitromethylene)-1-((tetrahydrofuran-3-yl)methyl) imidazolidine

2.5 g (0.0178 mol) of 1,1-dimethylthio-2-nitroethene, 2.56 g (0.0178 mol) of N¹-((tetrahydrofuran-3-yl)methyl)ethane-1,2-diamine were added to 50 ml of ethanol. The resulting mixture was heated under reflux for 8 hours at 80-90 ° C. The mixture was then cooled to educe solid, concentrated, filtrated and dried to give a light yellow powder in 81% yield.

GC MS (m/s) 177(29), 99(100), 56(9).

(3): Synthesis of 8-nitro-1-((tetrahydrofuran-3-yl)methyl)-1,2,3,5,6,7-hexahydro imidazo[ 1,2-a]pyridin-5-ol

A mixture of 0.002 mol of 2-(nitromethylene)-1-((tetrahydrofuran-3-yl)methyl)imidazolidine, 15 ml of anhydrous acetonitrile, 0.15 ml of acrylaldehyde and a catalytic amount of HCl place in a 50 ml of flask was heated to 40° C. and the mixture was kept at 40° C. and stirred for 12 hours. The reaction was stopped and the solvent was removed to obtain a crude solid. After recrystallization, the pure product, which was a light yellow powder, was obtained in 67% yield.

Mp=144.2-146.1 ° C.

IR (KBr, cm⁻¹) 3194, 1564, 1545, 1373, 1300, 1310, 1293, 1150.

Elementary analysis Calculated: C53.52, H 7.11, N 15.60; found C 53.78, H 7.12, N 15.35

EXAMPLE 12 Synthesis of 8-nitro-5-propoxy-1-((tetrahydrofuran-3-yl)methyl)-1,2,3,5,6,7-hexahydroimidazo[1,2-a]pyridine (compound 12)

0.001 mol of compound 11 was added to a 50 ml of round-bottomed flask, and 15 ml of propanol and a catalytic amount of glacial acetic acid were added. The resulting mixture was refluxed and followed by TLC. After the reaction was stopped, the solvent was removed. The residue was then separated to give a pure yellow powder by column chromatography in 85% yield.

Mp=96.4-97.2° C.

IR (KBr) 3052 m, 2872 m, 1573 vs, 1503s, 1312 vs, 1300 m, 1297 vs, 1150 vs, 1030s cm⁻¹

Elementary analysis Calculated: C 57.86, H 8.09, N 13.49; found C 58.04, H 7.97, N 13.42

EXAMPLE 13 Synthesis of 1-((6-chloropyridin-3-yl)methyl)-8-nitro-1,2,3,5,6,7-hexahydro imidazo[1,2-a]pyridin-5-yl acetate (compound 13)

0.001 mol of compound 1 was added to a 50 ml of round-bottomed flask, and, 0.001 mol of acetic anhydride and 0.001 mol of pyridine were added. The resulting mixture was stirred at room temperature and followed by TLC. After the reaction was stopped, the solvent was removed. Then the residue was separated to give a pure light yellow powder by column chromatography in 70% yield.

Mp=134-134.7° C.

IR (KBr cm⁻¹) 2903, 2370, 1713, 1332, 1203, 1123, 1071, 1000, 973, 830, 592

¹HNMR (CDCl₃) δ (ppm) 500 MHz: 8.33(d, J=2 Hz, 1H, Py-H), 7.88(dd, J₁=2 Hz, J₂ =8 Hz, 1H, Py-H), 7.36(d, J=8 Hz, 1H, Py-H), 4.79(d, J₁=15 Hz, J₂=15 Hz, 2H, —CH₂—N—), 4.48(t, J₁=3 Hz,J₂=3 Hz, 1H, —CHO—), 4.12(m, 3H, —OCOCH₃), 3.62(m, 4H, imidazolidine-H), 2.97(m, 2H, —CH₂CH₂—), 2.12(m, 2H, —CH₂CH₂—).

Elementary analysis Calculated: C 51.07, H 4.86, N 15.88; found C 51.23 H 4.88, N 15.92

EXAMPLE 14 Synthesis of 1-((6-chloropyridin-3-yl)methyl)-5-(ethylthio)-8-nitro-1,2,3,5,6,7-hexahydroimidazo[1,2-a]pyridine (compound 14)

0.31 g (0.001 mol) of compound 1 was added to a 50 ml of round-bottomed flask, and 15 ml of ethanethiol and a catalytic amount of Boron trifluoride dissolved in tetrahydrofuran were added. The resulting mixture was refluxed and followed by TLC. After the reaction was stopped, the solvents were removed. The residue was then separated to give a pure yellow powder by column chromatography in 90% yield.

Mp=167.2-168.3° C.; IR (KBr, cm⁻¹) 2902, 1563, 1350, 1078, 900, 760, 590

¹HNMR (CDCl₃) δ (ppm) 500 MHz: 8.31(d, J=2 Hz, 1H, Py-H), 7.89(dd, J₁=2 Hz, J₂ =8Hz, 1H, Py-H), 7.35(d, J=8 Hz, 1H, Py-H), 4.71(d, J₁=15 Hz, J₂=15 Hz, 2H, —CH₂—N—), 4.32(t, J₁=3 Hz,J₂=3 Hz, 1H, —CHO—), 3.60(m, 4H, imidazolidine-H), 2.89(m, 3H, —SCH₃), 2.90(m, 2H, —CH₂CH₂—), 1.91(m, 2H, —CH₂CH₂—)

Elementary analysis Calculated: C 49.34,H 5.03,N 16.44; found C 48.98,H 5.23,N 16.48

EXAMPLE 15 Synthesis of (E)-1-((6-chloropyridin-3-yl)methyl)-8-nitro-2,3,6,7-tetrahydro imidazo[1,2-a]pyridin-5(1H)-one oxime (1): Synthesis of 1-((6-chloropyridin-3-yl)methyl)-8-nitro-2,3,6,7-tetrahydro imidazo[1,2-a]pyridin-5(1H)-one

A mixture of 0.509 g (0.002 mol) of 2-chloro-5-((2-(nitromethylene)imidazolidin-1-yl) methyl)pyridine, 15 ml of anhydrous methanol and 0.002 mol methyl acrylate placed in a 50 ml of flask was refluxed for 30 hours and then separated to give a product by column chromatography in 40% yield.

Mp=167.0-168.1° C.

IR (KBr, cm⁻¹) 3190, 1685, 1612

MS: m/z=308.

(2): Synthesis of (E)-1-((6-chloropyridin-3-yl)methyl)-8-nitro-2,3,6,7-tetrahydro imidazo[1,2-a]pyridin-5(1H)-one oxime

A mixture of 0.618 g (0.002 mol) of 1-((6-chloropyridin-3-yl)methyl)-8-nitro-2,3,6,7-tetrahydroimidazo[1,2-a]pyridin-5(1H)-one, 0.01 mol of hydroxylamine hydrochloride, 0.01 mol of potassium hydroxide and 20 ml of ethanol placed in a 100 ml of flask was refluxed for 24 hours. The solvent was removed and the residue was separated to give a product by column chromatography in 65% yield.

Mp=189.1-190.3° C.

¹HNMR (CDCl₃) δ (ppm) 500 MHz: 8.34(d, J=2Hz, 1H, Py-H), 7.89(dd, J₁=2 Hz, J₂=8 Hz, 1H, Py-H), 7.41(d, J=8 Hz, 1H, Py-H), 4.79(d, J₁=15 Hz, J₂=15 Hz, 2H, —CH₂—N—), 3.62(m, 4H, imidazolidine-H), 3.97(m, 2H, —CH₂CH₂—), 2.96(m, 2H, —CH₂CH₂—)

Elementary analysis Calculated: C 48.23,H 4.36,N 21.63; found C 48.02,H 4.42,N 21.92

EXAMPLE 16 Synthesis of (E)-1-((6-chloropyridin-3-yl)methyl)-8-nitro-2,3,6,7-tetrahydro imidazo [1,2-a]pyridin-5(1H)-one 0-methyl oxime (compound 16)

The mixture of 0.002 mol of compound 15, 0.002 mol of sodium methoxide, 0.002 mol of methyl iodide and 20 ml of methanol placed in a 100 ml of flask was stirred at room temperature for 20 hours, evaporated to remove solvent and then separated to give a pure product by column chromatography in 56% yield. Mp=156.2-156.7° C.

¹HNMR (CDCl₃) δ (ppm)500 MHz: 8.35(d, J=2 Hz, 1H, Py-H), 7.90(dd, J₁=2 Hz, J₂ =8 Hz, 1H, Py-H), 7.39(d, J=8 Hz, 1H, Py-H), 4.78(d, J₁=15 Hz, J₂=15 Hz, 2H, —CH₂—N—), 3.62(m, 4H, imidazolidine-H), 3.99(m, 2H, —CH₂CH₂—), 3.69(s, 1H, —OCH₃), 2.93(m, 2H, —CH₂CH₂—). Elementary analysis Calculated: C 49.78,H 4.77,N 20.73; found C 40.89,H 4.69,N 21.21

EXAMPLE 17-227

According to a similar method described in example 1-16,the compound Nos. 17-227 in table 1 were obtained using proper starting materials.

The compound of the present invention can be used to control and kill general insects, including sucking insects, biting insects and other plant parasite, storage cereal insects and health hazard insects.

The examples of insects are listed as follow:

Coleoptera: Sitophilus zeamais, Tribolium castaneum, Henosepilachna vigintioctomaculata, Agriotes fuscicollis, Monolepta hieroglyphica, Diabrotica SPP, Anomala cupripes, Monochamus alternatus, Echinocnemus squameus, Lyrtus hrunneus

Lepidoptera: Lymantria dispar, Malacosoma neustria testacea, Prodenia litura, Mamestra brassicae, Chilo stuppressalis, Ostrinia nubilalis, Cadra cautella, Adoxophyes orana, Laspeyresia splendana, Agrotis fucosa, Galleria mellonella, Plutella xylostella, Phyllocnistis citrella

Hemiptera: Nephotettix cincticeps, Nilaparvata lugens, Pseudococcus comstocki, Unaspis yanonensis, Myzus persicae, Aphis pomi, Lipaphis erysimi pseudobrassicae, Stephanitis nashi, Nazara SPP, Cimicidae, Trialeurodes vaporariorum, and Psylle SPP.

Orthoptera: Blattella germanica, Periplaneta americana, Gryllotalpa africana, Locusta migratoria.

Isoptera: Deucotermes speratits, Coptotermes formosanus

Diptera: Musca domestica, Aedes aegypti, Hylemya platura, Delia platura, Anopheles sinensi.

The compounds in this invention have special effects to insects having a piercing-sucking or scratching mouthparts, such as aphid, leafhopper, planthopper, thrips, white fly.

These active compounds can be prepared into the customary formulations, such as solutions, emulsions, suspensions, powders, foams, pastes, granules, aerosols, natural and synthetic materials impregnated with active compounds, and micro-capsules in polymers used in the coating complex for seed, preparations used with a combustion device (such as smoking cylindrantherae, smoking can and smoking plate) and ULV cold mist and warm mist preparations. These formulations may be produced in a known manner, for example, by mixing the active compounds with extenders, which are liquid or liquefied gaseous or solid diluents or carriers, optionally with the use of surface-active agents, that is to say emulsifying agents and/or dispersing agents, and/or foam-forming agents. In the case of using water as an extender, organic solvents can, for example, also be used as auxiliary solvents

It is generally proper to use liquid solvents as a diluent or carrier, for example, aromatic hydrocarbons, such as xylene, toluene and alkyl naphthalenes, chlorinated aromatic or chlorinated aliphatic hydrocarbons, such as chlorobenzenes, chloroethylenes and methylene chloride, aliphatic hydrocarbons, such as cyclohexane or paraffins, for example, mineral oil fractions, alcohols, such as butanol or glycol as well as their ethers and esters, ketones, such as acetone, methyl ethyl ketone, methyl isobutyl ketone or cyclohexanone, or uncommon polar solvents, such as dimethylformamide and dimethylsulfoxide, as well as water.

By liquefied gaseous diluents or carriers are meant liquids which are gaseous at normal temperature and under normal pressure, for example, aerosol propellants, such as halogenated hydrocarbons as well as butane, propane, nitrogen and carbon dioxide.

The solid carrier can use ground natural minerals, such as kaolins, clays, talcs, quartzs, attapulgites, montmorillonites or kieselguhrs; ground synthetic minerals, such as high-dispersed silicic acid, alumina and silicate. The solid carrier used for particles is crushed and fractionated natural rocks such as calcite, marble, pumice, sepiolite and dolomite, as well as synthetic granules of inorganic and organic coarse powder, and granules of organic material such as sawdust, coconut shells, maize cobs and tobacco stalks and the like.

Nonionic and anionic emulsifiers may be used as emulsifying and/or foam-forming agents, such as polyoxyethylene-fatty acid esters, polyoxyethylene-fatty alcohol ethers, for example, alkylaryl polyglycol ethers, alkylsulfonates, alkylsulfates, arylsulfonates as well as albumin hydrolysis products. Dispersing agents include, for example, lignin sulfite waste liquors and methylcellulose.

Adhesives such as carboxymethyl cellulose and natural and synthetic polymers, (such as gum arabic, polyvinyl alcohol and polyvinyl acetate) in the form of powders, granules or emulsions can be used in the formulations

It is possible to use colorants such as inorganic dyestuffs, for example, iron oxide, cobalt oxide and Prussian Blue, and organic dyestuffs, such as diazo dyestuffs or metal phthalo-cyanine dyestuffs, and trace nutritional agent, such as the salts of iron, manganese, boron, copper, cobalt, aluminum and zinc.

The formulations, in general, contain from 0.01 to 99.99 percent by weight of active compound, preferably 0.1-99.wt %, more preferably 0.5-90.wt %.

The active compound of the present invention can be present as a mixture with other active compounds in a commercial formulation or a use form prepared from the commercial formulation. The other compound can be insecticide, bactericide, acaricide, nematocide, fungicide, growth controller and the like. The insecticide includes phosphates, carbamate, pyrethroids, chlorinated hydrocarbons, benzoylurea, nereistoxin and material produced by microbion such as avermectin.

Furthermore, the active compound of the present invention can be present as a mixture with a synergist in a commercial formulation or a use form prepared from the commercial formulation. Synergist is used to enhance the action of active compound, so if the compound itself is active there is no need to use it.

The concentration of the active compound in the use form prepared from the commercial formulation can vary within a wide range. The active compound concentration of the formulation for use is, for example, from 0.0000001 to 100 percent by weight of active compound, preferably from 0.0001 to 1 percent by weight.

These compounds can be prepared into proper dosage forms and used by common methods

Activity Test

Test on the insecticidal activity of Compound Nos. 1-227

Aphis, which belongs to Homoptera and has a piercing-sucking mouthpart, is a common insect for agricultural plant. Aphis craccivoral was tested by the way of immersing.

Test method: exactly weighed various samples were independently added to N,N-dimethylformamide to form a 10 g/L stock solution. The mixture was diluted with 0.2 mL/L aqueous Triton X-100 solution to a concentration of 500 ug/mL. After stably sucking on bean sprout, the adult aphis without wings together with bean sprout was dipped into 500 ug/mL dilution, taken out after 5 seconds, and the excess dilution was sucked out with bibulous paper and the adult aphis without wings was incubated in clean vessel at a constant temperature of 23° C. Each concentration was repeated for 3 times and the control group contained 0.2 mL/L aqueous Triton X-100 solution. The number of killed aphis was counted after 24 hours to calculate the mortality. The result was shown in Table 1 bellow

Planthopper, which belongs to Homoptera and has a piercing-sucking mouthpart, is a common insect for agricultural plant. Nilaparvata lugens was tested by the way of spraying.

Test method: the test compound was exactly formulated into a solution having a certain concentration and clean water was used as a blank control. Each process was repeated for 3 tumblers (3 times). 2 ml of solution was sprayed uniformly to each tumbler by a mini manual sprayer. 10 Nilaparvata lugens were introduced to every sink 6 hours before spraying. Three series of experiments were conducted. The number of killed Nilaparvata lugens was counted after 24 hours to calculate the mortality. The result was shown in Table 1 bellow. TABLE 1

mortality (%) (500 ppm) Nilapar- Compound Melting point vata- number R₁ R₂ R₃ R₄ A n (° C.) Aphis lugens 1

H H H —O 0 169-172 96 100 2

CH₃ H H —O 0 154-155 100 100 3

CH₂CH₃ H H —O 0 126-128 100 100 4

CH₂CH₂Cl H H —O 0 158-159 76 100 5

CH₂CF₃ H H —O 0 112-113 100 100 6

CH₂CH₂CH₃ H H —O 0 115-117 100 100 7

CH(CH₃)₂ H H —O 0 130-134 100 100 8

CH₂(CF₃)₂ H H —O 0 98-99 80 100 9

CH₂(CH₂)₂CH₃ H H —O 0 104-106 76 97 10

CH₂CH(CH₃)₂ H H —O 0 115-116 100 100 11

CH(CH₃)CH₂CH₃ H H —O 0 116-117 36 86 12

C(CH₃)₃ H H —O 0 145-147 100 100 13

C(CH₃)₂CCl₃ H H —O 0 192-193 56 90 14

CH₂(CH₂)₃CH₃ H H —O 0 83-85 52 100 15

CH₂CH₂CH(CH₃)₂ H H —O 0 110-111 67 97 16

CH(CH₃)(CH₂)₂CH₃ H H —O 0 125-126 89 100 17

CH₂C(CH₃)₃ H H —O 0 168-170 100 100 18

H H —O 0 136-137 23 67 19

CH₂CH═CH₂ H H —O 0 146-147 35 78 20

CH₂C═CH H H —O 0 168-169 39 56 21

CH₂CH₂OCH₃ H H —O 0 117-118 100 100 22

CH₂CH₂OCH₂CH₃ H H —O 0 108-109 100 100 23

H H H —O 0 172-174 87 100 24

CH₃ H H —O 0 150-151 100 100 25

CH₂CH₃ H H —O 0 128-129 100 100 26

CH₂CH₂Cl H H —O 0 161-162 26 64 27

CH₂CF₃ H H —O 0 115-116 100 100 28

CH₂CH₂CH₃ H H —O 0 117-119 100 100 29

CH(CH₃)₂ H H —O 0 133-135 100 100 30

CH₂(CF₃)₂ H H —O 0 98-99 58 98 31

CH₂(CH₂)₂CH₃ H H —O 0 104-106 56 35 32

CH₂CH(CH₃)₂ H H —O 0 115-116 37 23 33

CH(CH₃)CH₂CH₃ H H —O 0 116-117 24 56 34

C(CH₃)₃ H H —O 0 145-147 100 100 35

C(CH₃)₂CCl₃ H H —O 0 189-190 98 100 36

CH₂(CH₂)₃CH₃ H H —O 0 87-89 34 57 37

CH₂CH₂CH(CH₃)₂ H H —O 0 111-112 56 64 38

CH(CH₃)(CH₂)₂CH₃ H H —O 0 127-129 35 67 39

CH₂C(CH₃)₃ H H —O 0 169-170 24 35 40

H H —O 0 141-142 45 67 41

CH₂CH═CH₂ H H —O 0 152-154 89 100 42

CH₂C≡CH H H —O 0 171-172 45 100 43

CH₂CH₂OCH₃ H H —O 0 117-119 100 100 44

CH₂CH₂OCH₂CH₃ H H —O 0 112-114 67 100 45

H H H —O 0 144-146 56 89 46

CH₃ H H —O 0 130-131 100 100 47

CH₂CH₃ H H —O 0 101-102 45 100 48

CH₂CH₂Cl H H —O 0 127-129 3 0 49

CH₂CF₃ H H —O 0 97-98 45 32 50

CH₂CH₂CH₃ H H —O 0 96-97 100 100 51

CH(CH₃)₂ H H —O 0 108-109 34 23 52

CH₂(CF₃)₂ H H —O 0 82-83 34 12 53

CH₂(CH₂)₂CH₃ H H —O 0 96-98 9 12 54

CH₂CH(CH₃)₂ H H —O 0 101-102 23 34 55

CH(CH₃)CH₂CH₃ H H —O 0 111-112 45 12 56

C(CH₃)₃ H H —O 0 123-125 100 100 57

C(CH₃)₂CCl₃ H H —O 0 181-184 34 38 58

CH₂(CH₂)₃CH₃ H H —O 0 68-70 34 23 59

CH(CH₃)CH₂CH₃ H H —O 0 98-99 2 3 60

CH₂CH₂CH(CH₃)₂ H H —O 0 113-115 3 5 61

CH(CH₃)(CH₂)₂CH₃ H H —O 0 121-122 56 89 62

CH₂C(CH₃)₃ H H —O 0 136-137 12 23 63

H H —O 0 121-125 2 6 64

CH₂CH═CH₂ H H —O 0 135-137 37 46 65

CH₂C≡CH H H —O 0 156-157 47 34 66

CH₂CH₂OCH₃ H H —O 0 117-118 100 100 67

CH₂CH₂OCH₂CH₃ H H —O 0 98-99 100 100 68

H Me H —O 0 146-147 2 7 69

H Me H —O 0 164-165 45 56 70

H Me H —O 0 165-166 33 12 71

H H H —O 1 172-173 6 0 72

CH₃ H H —O 1 156-157 35 100 73

CH₂CH₃ H H —O 1 129-130 34 56 74

CH₂CH₂Cl H H —O 1 160-161 12 13 75

CH₂CF₃ H H —O 1 114-115 88 100 76

CH₂CH₂CH₃ H H —O 1 118-119 100 100 77

CH(CH₃)₂ H H —O 1 135-137 56 78 78

CH₂(CF₃)₂ H H —O 1 102-103 68 51 79

CH₂(CH₂)₂CH₃ H H —O 1 114-115 52 61 80

CH₂CH(CH₃)₂ H H —O 1 124-126 23 34 81

CH(CH₃)CH₂CH₃ H H —O 1 127-128 12 8 82

C(CH₃)₃ H H —O 1 195-197 12 34 83

CH₂CH₂OCH₃ H H —O 1 167-168 38 26 84

CH₂CH₂OCH₂CH₃ H H —O 1 169-170 26 39 85

H H H —O 1 175-176 12 23 86

CH₃ H H —O 1 158-159 100 100 87

CH₂CH₃ H H —O 1 128-130 100 100 88

CH₂CH₂Cl H H —O 1 165-168 23 34 89

CH₂CF₃ H H —O 1 119-120 100 100 90

CH₂CH₂CH₃ H H —O 1 123-125 34 51 91

CH(CH₃)₂ H H —O 1 138-139 69 71 92

CH₂(CF₃)₂ H H —O 1 112-116 6 5 93

CH₂(CH₂)₂CH₃ H H —O 1 118-119 7 8 94

CH₂CH(CH₃)₂ H H —O 1 128-129 8 3 95

CH(CH₃)CH₂CH₃ H H —O 1 131-133 4 8 96

C(CH₃)₃ H H —O 1 199-200 80 100 97

CH₂CH₂OCH₃ H H —O 1 169-170 78 100 98

CH₂CH₂OCH₂CH₃ H H —O 1 165-167 4 7 99

H H H —O 1 162-163 6 7 100

CH₃ H H —O 1 143-145 3 8 101

CH₂CH₃ H H —O 1 113-112 76 90 102

CH₂CH₂Cl H H —O 1 146-148 0 89 103

CH₂CF₃ H H —O 1 102-103 6 100 104

CH₂CH₂CH₃ H H —O 1 108-109 3 24 105

CH(CH₃)₂ H H —O 1 117-119 10 98 106

CH₂(CF₃)₂ H H —O 1 98-99 45 100 107

CH₂(CH₂)₂CH₃ H H —O 1 104-106 7 0 108

CH₂CH(CH₃)₂ H H —O 1 109-111 1 9 109

CH(CH₃)CH₂CH₃ H H —O 1 113-115 2 10 110

C(CH₃)₃ H H —O 1 178-179 67 98 111

H H —O 0 187-189 1 23 112

H H —O 0 193-195 38 75 113

COCH₃ H H —O 0 167-169 45 77 114

COCH₂CH₃ H H —O 0 165-166 56 88 115

COCCl₃ H H —O 0 194-196 0 33 116

COCF₃ H H —O 0 135-137 2 45 117

SO₂CH₃ H H —O 0 178-179 19 65 118

SO₂CF₃ H H —O 0 167-168 81 100 119

H H —O 0 196-197 3 23 120

H H —O 0 182-184 1 5 121

H H —O 0 183-185 0 8 122

H H —O 0 176-178 56 23 123

H H —O 0 176-177 56 100 124

H H —O 0 183-186 22 0 125

H H —O 0 156-158 67 92 126

H H —O 0 178-179 93 100 127

H H —O 0 180-181 45 78 128

H H —O 0 193-195 0 21 129

H H —O 0 196-197 0 34 130

H H —O 0 201-202 23 67 131

H H —O 0 197-199 3 0 132

CH₃ H H —S 0 167-168 100 100 133

CH₂CH₃ H H —S 0 145-147 100 100 134

CH₂CH₂Cl H H —S 0 178-179 34 78 135

CH₂CF₃ H H —S 0 156-158 98 100 136

CH₂CH₂CH₃ H H —S 0 136-138 100 100 137

CH(CH₃)₂ H H —S 0 151-152 89 100 138

CH₂(CF₃)₂ H H —S 0 137-138 45 98 139

CH₂(CH₂)₂CH₃ H H —S 0 124-125 34 78 140

CH₂CH(CH₃)₂ H H —S 0 135-138 67 78 141

CH(CH₃)CH₂CH₃ H H —S 0 139-140 56 89 142

C(CH₃)₃ H H —S 0 160-161 67 88 143

CH₂(CH₂)₃CH₃ H H —S 0 112-113 23 34 144

CH(CH₃)CH₂CH₃ H H —S 0 128-129 12 56 145

CH₂CH₂CH(CH₃)₂ H H —S 0 131-132 67 78 146

CH(CH₃)(CH₂)₂CH₃ H H —S 0 129-130 35 97 147

CH₂C(CH₃)₃ H H —S 0 138-139 56 99 148

CH₂CH₂OCH₃ H H —S 0 128-129 67 89 149

CH₂CH₂OCH₂CH₃ H H —S 0 126-127 98 100 150

H H —O 0 186-187 3 67 151

H H —O 0 197-199 2 16 152

COCH₃ H H —O 0 169-170 3 0 153

COCH₂CH₃ H H —O 0 168-169 29 38 154

COCCl₃ H H —O 0 197-198 93 100 155

COCF₃ H H —O 0 138-139 48 90 156

SO₂CH₃ H H —O 0 178-180 78 92 157

SO₂CF₃ H H —O 0 169-171 56 100 158

H H —O 0 198-199 6 7 159

H H —O 0 186-187 0 8 160

H H —O 0 187-189 4 8 161

H H —O 0 177-178 3 5 162

H H —O 0 179-180 34 98 163

H H —O 0 187-188 1 0 164

H H —O 0 163-165 59 78 165

H H —O 0 184-188 90 100 166

H H —O 0 185-188 0 45 167

H H —O 0 193-194 12 4 168

H H —O 0 198-199 56 100 169

H H —O 0 207-209 2 13 170

H H —O 0 195-196 2 0 171

CH₃ H H —S 0 169-170 97 100 172

CH₂CH₃ H H —S 0 148-149 100 100 173

CH₂CH₂Cl H H —S 0 179-181 45 56 174

CH₂CF₃ H H —S 0 159-161 67 100 175

CH₂CH₂CH₃ H H —S 0 139-140 89 100 176

CH(CH₃)₂ H H —S 0 155-156 78 98 177

CH₂(CF₃)₂ H H —S 0 141-142 56 65 178

CH₂(CH₂)₂CH₃ H H —S 0 127-128 23 12 179

CH₂CH(CH₃)₂ H H —S 0 138-139 12 56 180

CH(CH₃)CH₂CH₃ H H —S 0 142-143 34 78 181

C(CH₃)₃ H H —S 0 166-167 45 78 182

CH₂(CH₂)₃CH₃ H H —S 0 117-119 67 87 183

CH₂CH₂CH(CH₃)₂ H H —S 0 136-137 23 34 184

CH(CH₃)(CH₂)₂CH₃ H H —S 0 131-132 12 35 185

CH₂C(CH₃)₃ H H —S 0 143-144 36 86 186

CH₂CH₂OCH₃ H H —S 0 132-133 97 100 187

CH₂CH₂OCH₂CH₃)₃ H H —S 0 127-129 34 97 188

H H H ═N 0 189-190 55 67 189

CH₃ H H ═N 0 156-157 100 100 190

CH₂CH₃ H H ═N 0 146-147 89 100 191

CH₂CH₂Cl H H ═N 0 176-177 53 78 192

CH₂CH₂CH₃ H H ═N 0 125-127 86 100 193

CH(CH₃)₂ H H ═N 0 137-137 93 98 194

CH₂CH₂CH₂CH₃ H H ═N 0 118-119 34 45 195

CH₂(CH₂)₃CH₃ H H ═N 0 101-102 46 78 196

CH₂CH₂CH(CH₃)₂ H H ═N 0 123-124 12 25 197

CH(CH₃)(CH₂)₂CH₃ H H ═N 0 131-132 8 56 198

CH₂C(CH₃)₃ H H ═N 0 143-144 39 89 199

CH₂CH₂OCH₃ H H ═N 0 121-123 16 36 200

CH₂CH₂OCH₂CH₃)₃ H H ═N 0 119-120 45 78 201

H H H ═N 1 193-194 54 55 202

CH₃ H H ═N 1 163-165 89 98 203

CH₂CH₃ H H ═N 1 151-155 92 100 204

CH₂CH₂Cl H H ═N 1 178-179 46 78 205

CH₂CH₂CH₃ H H ═N 1 128-129 35 100 206

CH(CH₃)₂ H H ═N 1 139-140 56 98 207

CH₂CH₂CH₂CH₃ H H ═N 1 120-122 14 45 208

CH₂(CH₂)₃CH₃ H H ═N 1 104-106 35 67 209

CH₂CH₂CH(CH₃)₂ H H ═N 1 126-127 23 26 210

CH(CH₃)(CH₂)₂CH₃ H H ═N 1 135-136 7 77 211

CH₂C(CH₃)₃ H H ═N 1 147-148 34 56 212

H H H ═N 0 203-205 34 23 213

CH₃ H H ═N 0 169-170 32 78 214

CH₂CH₃ H H ═N 0 157-158 55 90 215

CH₂CH₂Cl H H ═N 0 182-183 9 97 216

CH₂CH₂CH₂CH₃ H H ═N 0 136-138 66 98 217

CH₂CH₂CH₃ H H ═N 0 145-146 23 100 218

CH₂(CH₂)₃CH₃ H H ═N 0 129-130 45 67 219

CH(CH₃)₂ H H ═N 0 142-145 34 45 220

H H H ═N 1 205-207 16 56 221

CH₃ H H ═N 1 172-176 4 67 222

CH₂CH₃ H H ═N 1 162-163 4 89 223

CH₂CH₂Cl H H ═N 1 185-186 5 76 224

CH₂CH₂CH₂CH₃ H H ═N 1 137-138 45 66 225

CH₂CH₂CH₃ H H ═N 1 147-148 35 78 226

CH₂(CH₂)₃CH₃ H H ═N 1 133-135 22 57 227

CH(CH₃)₂ H H ═N 1 146-148 100 100

COMPOSITION EXAMPLE 1

(a) Oily Suspension Any one of compounds 1-16 25 wt % Polyoxyethylene sorbital hexaoleate  5 wt % Higher aliphatic hydrocarbon oil 70 wt %

Each of the components was ground in a sand mill until the solid granules were reduced to less than about 5 micrometer. The resulting viscous suspension can be used directly or may be used after it was emulsified in water.

(b) Aqueous Suspension Any one of compounds 1-16 25 wt % Hydrate attapulagit  3 wt % Calcium lignosulphonate 10 wt % Sodium dihydrogen phosphate 0.5 wt %  Water 61.5 wt %  

Each of the components was ground in a ball mill until the solid granules were reduced to less than about 10 micrometer. The aqueous suspension can be used directly.

All the documents cited herein are incorporated into the invention as reference, as if each of them is individually incorporated. Further, it would be appreciated that, in light of the above described teaching of the invention, the skilled in the art could make various changes or modifications to the invention, and these equivalents would still be within the scope of the invention defined by the appended claims of the application. 

1. A derivative of the following formula,

or an agriculturally acceptable salt thereof, wherein R₁ represents a substituted or unsubstituted 5- or 6-membered heterocyclyl containing nitrogen, oxygen and/or sulfur, wherein the substituents are one to three substituents selected from the group consisting of a halogen atom, C₁₋₄ haloalkyl and C₁₋₄ haloalkoxyl; R₂ represents a hydrogen atom, a saturated or unsaturated C₁₋₈ hydrocarbyl group, a saturated or unsaturated C₁₋₈ halogenated hydrocarbyl group, —CH₂CH₂OCH₂CH₃, —CH₂CH₂OCH₃, a substituted or unsubstituted phenyl group, a substituted or unsubstituted benzyl group, a substituted or unsubstituted C₁-₈ alkoxyl group which is saturated or unsaturated, wherein the substituents are one to three substituents selected from the group consisting of halogen, C₁₋₄ haloalkyl and C₁₋₄ haloalkoxyl; or R₂ represents a group of the following formula:

wherein Ra represents a methyl group, a trifluoromethyl group or a phenyl group; Rb represents a methyl group, a trifluoromethyl group, a pyridyl group, a phenyl group or a phenyl group substituted with a halogen atom and/or a nitro group; R₃ and R₄ independently represents a hydrogen atom, a substituted or unsubstituted C₁₋₃ alkyl group, wherein the substituents are one to three substituents selected from the group consisting of a halogen atom, C₁₋₄ haloalkyl and C₁₋₄ haloalkoxyl; A represents O, S or N; and n represents 0 or
 1. 2. The derivative according to claim 1, wherein R₁ represents a pyridyl group, a thiazolyl group, a pyrimidinyl group, a tetrahydrofuryl group, an oxazolyl group, or the chlorides thereof.
 3. The derivative according to claim 2, wherein R₁ represents


4. The derivative according to claim 1, wherein R₂ represents a hydrogen atom, a saturated or unsaturated C₁₋₈ hydrocarbyl group, a saturated or unsaturated C₁₋₈ halogenated hydrocarbyl group, —CH₂CH₂OCH₂CH₃, —CH₂CH₂OCH₃, or a saturated or unsaturated C₁₋₈ alkoxyl group.
 5. The derivative according to claim 1 which has the structure of formula II

wherein R₁, R₂ and A are defined as above.
 6. The derivative according to claim 1, wherein R₄ represents a hydrogen atom or a C₁₋₃ alkyl group.
 7. The derivative according to claim 1, wherein R₃ represents a hydrogen atom or a methyl group.
 8. The derivative according to claim 1, wherein the derivative is compound Nos. 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15 or
 16. 9. The use of the derivative according to any of claims 1-8 in the preparation of a chemical insecticide for agriculture.
 10. An insecticidal composition comprising an effective amount of a derivative according to claim 1 or an agriculturally acceptable salt thereof in mixture with an agriculturally acceptable carrier or diluent. 